Sodium Methoxide → 5-(2-(Methylthio)ethoxy)pyrimidin-2-amine

HRID 1442505노트

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HRID 1442505 반응식
[CH3:1][S:2][CH2:3][CH2:4][O:5][C:6]1[CH:7]=[N:8][C:9]([NH:12]C(=O)CCCCC)=[N:10][CH:11]=1.C[O-].[Na+]>CO>[CH3:1][S:2][CH2:3][CH2:4][O:5][C:6]1[CH:11]=[N:10][C:9]([NH2:12])=[N:8][CH:7]=1

참가 물질

4

실험 절차

N-{5-[2-(Methylthio)ethoxy]pyrimidin-2-yl}hexanamide (6.80 g, 24 mmol) was suspended in methanol (68 mL), the suspension was added with sodium methoxide (1 M solution in methanol, 120 mL, 120 mmol), the substances in the suspension were dissolved on an oil bath at 60° C., and the solution was stirred at the same temperature for 2 hours. The reaction mixture was concentrated under reduced pressure, the resulting residue was extracted with chloroform and water, and the organic layer was washed with saturated brine, dried over anhydrous sodium sulfate, and then concentrated under reduced pressure. The resulting residue was washed with ether-hexane, and taken by filtration to obtain 5-[2-(methylthio)ethoxy]pyrimidin-2-amine (2.93 g, 59%) as a pale yellow solid.

후처리

  1. dissolutionthe substances in the suspension were dissolved on an oil bath at 60° C.
  2. concentrationThe reaction mixture was concentrated under reduced pressure
  3. extractionthe resulting residue was extracted with chloroform and water
  4. washthe organic layer was washed with saturated brine
  5. dry with materialdried over anhydrous sodium sulfate
  6. concentrationconcentrated under reduced pressure
  7. washThe resulting residue was washed with ether-hexane
  8. filtrationtaken by filtration

출처 및 근거

ORD 기록
ord-b66d83fbb7e2433aa57672f39f7fb742
출처 데이터셋
uspto-grants-2010_02
특허 번호
US07659271B2

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